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Rest of Chapter 5 Human recombination studies Mapping by tetrad analysis in fungi Analysis of ordered tetrads Other features of recombination.
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Human pedigrees and mapping In humans, progeny numbers are small. Matings cannot be arranged for experiments. Coupling (AB/ab) vs. repulsion (Ab/aB) heterozygotes cannot be distinguished most of the time. Pedigrees can be pooled.
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Lod scores
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Fungi in genetic studies Haploid organisms can have genetic maps made by using spore analysis. No testcrosses are needed. (review of fungal biology)
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The life cycle of the baker’s yeast (Saccharomyces cerevisiae)
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Types of tetrads PD = parental ditype NPD = Nonparental ditype (no linkage, PD=NPD) (with linkage, PD>NPD) TT = Tetratype tetrad
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Tetrad analysis of unlinked genes using unordered asci For unlinked genes, parental ditype (PD) (having 2 kinds of spores) and nonparental ditype (NPD) asci are produced in equal proportion For unlinked genes, recombination between one of the genes and its centromere produces tetratype asci (TT) having 4 kinds of spores
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Tetrad analysis results for linked genes in unordered tetrads-1 No crossovers or 2-strand double crossovers result in parental ditype (PD) asci. One recombination between the genes results in tetratype (TT) asci
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Tetrad analysis results for linked genes in unordered tetrads-2 Three-strand double crossovers give the same result as a single crossover, tetratype asci (TT). Four- strand double crossovers give non-parental ditype (NPD) asci. As a result, for linked genes, PD >> NPD.
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Mapping with unordered tetrads: Map distance=(½)[TT]- 2[NPD]+4[NPD]/total ={(½)[TT]+3[NPD]/total # of tetrads }x 100
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A branch diagram for analyzing unordered tetrads data
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The life cycle of an ascomycete fungus with ordered tetrads
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Analysis of ordered tetrad data Ordered tetrads allow one to map the distance between a gene and its centromere. No crossover between a gene and its centromere gives first division segregation. A crossover between a gene and its centromere gives a second division segregation.
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Other types of recombination studies Recombination within genes Mitotic recombination
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Fine structure mapping allows mapping the internal structure of a locus. Cistron – defines one genetic function = mutations that fail to complement The term comes from cis and trans. Lozenge gene in Drosophila:
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X + lz BS + +++lz g v X X ___________ x _______________ > Y ct +lz g ct-lz=7.7 cM lz-v=5.3 cM 134 out of 16,000 progeny had normal eyes Frequency of recombination=0.008 What happened? X ct ++ + in all nonlozenge females and X + lz B Slz g v in 5 males with ‘new’ lz phenotype.
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Somatic recombination (mitotic crossover) can lead to twin spots
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